tert-Butyl 4-(chloromethyl)benzoate

95%

Reagent Code: #145344
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CAS Number 121579-86-0

science Other reagents with same CAS 121579-86-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.7 g/mol
Formula C₁₂H₁₅ClO₂
thermostat Physical Properties
Boiling Point 310°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. The compound serves as a building block for introducing the 4-(chloromethyl)benzoyl group into more complex molecules. The chloromethyl functionality allows for further alkylation or nucleophilic substitution reactions, making it valuable in the preparation of esters, amides, and other derivatives. It is also employed in the synthesis of functionalized polymers and in materials science where controlled substitution patterns on aromatic rings are required. Its tert-butyl ester group can be easily deprotected under mild acidic conditions, enabling selective transformations in multi-step syntheses.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10g
10-20 days ฿1,400.00
25g
10-20 days ฿3,160.00
100g
10-20 days ฿11,960.00
tert-Butyl 4-(chloromethyl)benzoate
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. The compound serves as a building block for introducing the 4-(chloromethyl)benzoyl group into more complex molecules. The chloromethyl functionality allows for further alkylation or nucleophilic substitution reactions, making it valuable in the preparation of esters, amides, and other derivatives. It is also employed in the synthesis of functionalized polymers and in materials science where controlled
Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. The compound serves as a building block for introducing the 4-(chloromethyl)benzoyl group into more complex molecules. The chloromethyl functionality allows for further alkylation or nucleophilic substitution reactions, making it valuable in the preparation of esters, amides, and other derivatives. It is also employed in the synthesis of functionalized polymers and in materials science where controlled substitution patterns on aromatic rings are required. Its tert-butyl ester group can be easily deprotected under mild acidic conditions, enabling selective transformations in multi-step syntheses.
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